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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

3-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]cyclobutanone

CC([Si](OC1CC(=O)C1)(C)C)(C)C Request for Quotation
Chemical Name: 3-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]cyclobutanone
CAS Number: 929913-18-8
Product Number: AG00IHF8(AGN-PC-0WAJXU)
Synonyms:
MDL No:
Molecular Formula: C10H20O2Si
Molecular Weight: 200.3501

Identification/Properties

Computed Properties
Molecular Weight:
200.353g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
200.123g/mol
Monoisotopic Mass:
200.123g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
208
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-((tert-Butyldimethylsilyl)oxy)cyclobutanone is a versatile compound widely used in chemical synthesis for its unique reactivity and structural properties. One key application of this compound is as a masked carbonyl synthon in organic chemistry. The tert-butyldimethylsilyl (TBDMS) protecting group attached to the ketone functionality provides stability and prevents undesired reactions during various synthetic transformations. Upon deprotection, the carbonyl group is revealed, allowing for further functional group interconversions or cyclization reactions.Additionally, 3-((tert-Butyldimethylsilyl)oxy)cyclobutanone can serve as a valuable building block for the construction of complex molecules due to its cyclobutane ring system, which can undergo ring-opening reactions to introduce additional functional groups or form fused ring systems. This compound's versatility makes it a valuable tool in the toolbox of synthetic chemists for the intricate design and synthesis of bioactive molecules or natural products.